← Back to catalogue

Humelock II Cementless Shoulder System

FDA UDI

Class I (US FDA UDI)

by Fx Solutions

Identity

Trade Name
Humelock II Cementless Shoulder System FDA UDI
Generic Name
Surgical instrument interim-placement holder, reusable FDA UDI
Device Name
HUMELOCK STEM HOLDER FDA UDI
Model / Reference
902-0021 FDA UDI
Description
HUMELOCK STEM HOLDER FDA UDI

Identifiers

Catalog Number
902-0021 FDA UDI
Primary DI / UDI-DI
03701037305614 FDA UDI
FDA Product Code
HXK FDA UDI
LXH FDA UDI
GMDN Term
Surgical instrument interim-placement holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic surgical procedure kit, non-medicated, reusableSurgical instrument interim-placement holder, reusable

Humelock II Cementless Shoulder System by Fx Solutions — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument interim-placement holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Fx Solutions

Sources (1)

  • FDA UDI 6d0a8866-f8f1-4685-8d9e-dfbead9db86d 35 fields · synced Jun 8, 2026